EUCTR2012-005337-37-IT进行中（未招募）不适用
ANTI-MULLERIAN HORMONE (AMH) AS A MARKER OF OVARIAN RESERVE IN YOUNG BREAST CANCER PATIENTS RECEIVING CHEMOTHERAPY + GnRH ANALOGUE
Istituto Clinico Humanitas0 个研究点开始时间: 2013年3月14日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •1)Female subjects, aged <40yr at the time of breast cancer diagnosis
- •2)Diagnosis of operable breast cancer any T and N, any ER
- •3)Patients candidate to adjuvant chemotherapy for 4-8 cycles.
- •4)Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements to be conducted within 28 days prior to the start of the study treatment.
- •5)Negative pregnancy test at the study enrolment; fertile women must use effective contraception during chemotherapy
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 80
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1)Presence of distant metastasis
- •2)Clinically significant cardiovascular disease
- •3)Psychological or social conditions which might affect study compliance
- •4)Unstable neurologic function
- •e)Patients with known allergy to any of the components of the study medication
- •5)Pregnancy or lactation
研究者
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